Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans
Schick, Ursula M., Jain, Deepti, Hodonsky, Chani J., Morrison, Jean V., Davis, James P., Brown, Lisa, Sofer, Tamar, Conomos, Matthew P., Schurmann, Claudia, McHugh, Caitlin P., Nelson, Sarah C., Vadlamudi, Swarooparani, Stilp, Adrienne, Plantinga, Anna, Baier, Leslie, Bien, Stephanie A., Gogarten, Stephanie M., Laurie, Cecelia A., Taylor, Kent D., Liu, Yongmei, Auer, Paul L., Franceschini, Nora, Szpiro, Adam, Rice, Ken, Kerr, Kathleen F., Rotter, Jerome I., Hanson, Robert L., Papanicolaou, George, Rich, Stephen S., Loos, Ruth J.F., Browning, Brian L., Browning, Sharon R., Weir, Bruce S., Laurie, Cathy C., Mohlke, Karen L., North, Kari E., Thornton, Timothy A., Reiner, Alex P.
Published in American journal of human genetics (04.02.2016)
Published in American journal of human genetics (04.02.2016)
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Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos
Hodonsky, Chani J, Jain, Deepti, Schick, Ursula M, Morrison, Jean V, Brown, Lisa, McHugh, Caitlin P, Schurmann, Claudia, Chen, Diane D, Liu, Yong Mei, Auer, Paul L, Laurie, Cecilia A, Taylor, Kent D, Browning, Brian L, Li, Yun, Papanicolaou, George, Rotter, Jerome I, Kurita, Ryo, Nakamura, Yukio, Browning, Sharon R, Loos, Ruth J F, North, Kari E, Laurie, Cathy C, Thornton, Timothy A, Pankratz, Nathan, Bauer, Daniel E, Sofer, Tamar, Reiner, Alex P
Published in PLoS genetics (28.04.2017)
Published in PLoS genetics (28.04.2017)
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Confirmation of the reported association of clonal chromosomal mosaicism with an increased risk of incident hematologic cancer
Schick, Ursula M, McDavid, Andrew, Crane, Paul K, Weston, Noah, Ehrlich, Kelly, Newton, Katherine M, Wallace, Robert, Bookman, Ebony, Harrison, Tabitha, Aragaki, Aaron, Crosslin, David R, Wang, Sophia S, Reiner, Alex P, Jackson, Rebecca D, Peters, Ulrike, Larson, Eric B, Jarvik, Gail P, Carlson, Christopher S
Published in PloS one (22.03.2013)
Published in PloS one (22.03.2013)
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Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities
Huang, Lam O, Rauch, Alexander, Mazzaferro, Eugenia, Preuss, Michael, Carobbio, Stefania, Bayrak, Cigdem S, Chami, Nathalie, Wang, Zhe, Schick, Ursula M, Yang, Nancy, Itan, Yuval, Vidal-Puig, Antonio, den Hoed, Marcel, Mandrup, Susanne, Kilpeläinen, Tuomas O, Loos, Ruth J F
Published in Nature metabolism (01.02.2021)
Published in Nature metabolism (01.02.2021)
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Understanding the complex genetic architecture connecting rheumatoid arthritis, osteoporosis and inflammation: discovering causal pathways
Kasher, Melody, Williams, Frances M K, Freidin, Maxim B, Malkin, Ida, Cherny, Stacey S, Livshits, Gregory
Published in Human molecular genetics (23.08.2022)
Published in Human molecular genetics (23.08.2022)
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Journal Article
Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos
Jain, Deepti, Hodonsky, Chani J, Schick, Ursula M, Morrison, Jean V, Minnerath, Sharon, Brown, Lisa, Schurmann, Claudia, Liu, Yongmei, Auer, Paul L, Laurie, Cecelia A, Taylor, Kent D, Browning, Brian L, Papanicolaou, George, Browning, Sharon R, Loos, Ruth J F, North, Kari E, Thyagarajan, Bharat, Laurie, Cathy C, Thornton, Timothy A, Sofer, Tamar, Reiner, Alexander P
Published in Human molecular genetics (15.03.2017)
Published in Human molecular genetics (15.03.2017)
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Journal Article
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis
Polfus, Linda M., Khajuria, Rajiv K., Schick, Ursula M., Pankratz, Nathan, Pazoki, Raha, Brody, Jennifer A., Chen, Ming-Huei, Auer, Paul L., Floyd, James S., Huang, Jie, Lange, Leslie, van Rooij, Frank J.A., Gibbs, Richard A., Metcalf, Ginger, Muzny, Donna, Veeraraghavan, Narayanan, Walter, Klaudia, Chen, Lu, Yanek, Lisa, Becker, Lewis C., Peloso, Gina M., Wakabayashi, Aoi, Kals, Mart, Metspalu, Andres, Esko, Tõnu, Fox, Keolu, Wallace, Robert, Franceschini, Nora, Matijevic, Nena, Rice, Kenneth M., Bartz, Traci M., Lyytikäinen, Leo-Pekka, Kähönen, Mika, Lehtimäki, Terho, Raitakari, Olli T., Li-Gao, Ruifang, Mook-Kanamori, Dennis O., Lettre, Guillaume, van Duijn, Cornelia M., Franco, Oscar H., Rich, Stephen S., Rivadeneira, Fernando, Hofman, Albert, Uitterlinden, André G., Wilson, James G., Psaty, Bruce M., Soranzo, Nicole, Dehghan, Abbas, Boerwinkle, Eric, Zhang, Xiaoling, Johnson, Andrew D., O’Donnell, Christopher J., Johnsen, Jill M., Reiner, Alexander P., Ganesh, Santhi K., Sankaran, Vijay G.
Published in American journal of human genetics (04.08.2016)
Published in American journal of human genetics (04.08.2016)
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Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits
Pankratz, Nathan, Schick, Ursula M, Zhou, Yi, Zhou, Wei, Ahluwalia, Tarunveer Singh, Allende, Maria Laura, Auer, Paul L, Bork-Jensen, Jette, Brody, Jennifer A, Chen, Ming-Huei, Clavo, Vinna, Eicher, John D, Grarup, Niels, Hagedorn, Elliott J, Hu, Bella, Hunker, Kristina, Johnson, Andrew D, Leusink, Maarten, Lu, Yingchang, Lyytikäinen, Leo-Pekka, Manichaikul, Ani, Marioni, Riccardo E, Nalls, Mike A, Pazoki, Raha, Smith, Albert Vernon, van Rooij, Frank J A, Yang, Min-Lee, Zhang, Xiaoling, Zhang, Yan, Asselbergs, Folkert W, Boerwinkle, Eric, Borecki, Ingrid B, Bottinger, Erwin P, Cushman, Mary, de Bakker, Paul I W, Deary, Ian J, Dong, Liguang, Feitosa, Mary F, Floyd, James S, Franceschini, Nora, Franco, Oscar H, Garcia, Melissa E, Grove, Megan L, Gudnason, Vilmundur, Hansen, Torben, Harris, Tamara B, Hofman, Albert, Jackson, Rebecca D, Jia, Jia, Kähönen, Mika, Launer, Lenore J, Lehtimäki, Terho, Liewald, David C, Linneberg, Allan, Liu, Yongmei, Loos, Ruth J F, Nguyen, Vy M, Numans, Mattijs E, Pedersen, Oluf, Psaty, Bruce M, Raitakari, Olli T, Rich, Stephen S, Rivadeneira, Fernando, Di Sant, Amanda M Rosa, Rotter, Jerome I, Starr, John M, Taylor, Kent D, Thuesen, Betina Heinsbæk, Tracy, Russell P, Uitterlinden, Andre G, Wang, Jiansong, Wang, Judy, Dehghan, Abbas, Huo, Yong, Cupples, L Adrienne, Wilson, James G, Proia, Richard L, Zon, Leonard I, O'Donnell, Christopher J, Reiner, Alex P, Ganesh, Santhi K
Published in Nature genetics (01.08.2016)
Published in Nature genetics (01.08.2016)
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Association of exome sequences with plasma C-reactive protein levels in >9000 participants
Schick, Ursula M, Auer, Paul L, Bis, Joshua C, Lin, Honghuang, Wei, Peng, Pankratz, Nathan, Lange, Leslie A, Brody, Jennifer, Stitziel, Nathan O, Kim, Daniel S, Carlson, Christopher S, Fornage, Myriam, Haessler, Jeffery, Hsu, Li, Jackson, Rebecca D, Kooperberg, Charles, Leal, Suzanne M, Psaty, Bruce M, Boerwinkle, Eric, Tracy, Russell, Ardissino, Diego, Shah, Svati, Willer, Cristen, Loos, Ruth, Melander, Olle, Mcpherson, Ruth, Hovingh, Kees, Reilly, Muredach, Watkins, Hugh, Girelli, Domenico, Fontanillas, Pierre, Chasman, Daniel I, Gabriel, Stacey B, Gibbs, Richard, Nickerson, Deborah A, Kathiresan, Sekar, Peters, Ulrike, Dupuis, Josée, Wilson, James G, Rich, Stephen S, Morrison, Alanna C, Benjamin, Emelia J, Gross, Myron D, Reiner, Alex P
Published in Human molecular genetics (15.01.2015)
Published in Human molecular genetics (15.01.2015)
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Journal Article
Rare coding variants and X-linked loci associated with age at menarche
Lunetta, Kathryn L., Day, Felix R., Sulem, Patrick, Ruth, Katherine S., Tung, Joyce Y., Hinds, David A., Esko, Tõnu, Elks, Cathy E., Altmaier, Elisabeth, He, Chunyan, Huffman, Jennifer E., Mihailov, Evelin, Porcu, Eleonora, Robino, Antonietta, Rose, Lynda M., Schick, Ursula M., Stolk, Lisette, Teumer, Alexander, Thompson, Deborah J., Traglia, Michela, Wang, Carol A., Yerges-Armstrong, Laura M., Antoniou, Antonis C., Barbieri, Caterina, Coviello, Andrea D., Cucca, Francesco, Demerath, Ellen W., Dunning, Alison M., Gandin, Ilaria, Grove, Megan L., Gudbjartsson, Daniel F., Hocking, Lynne J., Hofman, Albert, Huang, Jinyan, Jackson, Rebecca D., Karasik, David, Kriebel, Jennifer, Lange, Ethan M., Lange, Leslie A., Langenberg, Claudia, Li, Xin, Luan, Jian'an, Mägi, Reedik, Morrison, Alanna C., Padmanabhan, Sandosh, Pirie, Ailith, Polasek, Ozren, Porteous, David, Reiner, Alex P., Rivadeneira, Fernando, Rudan, Igor, Sala, Cinzia F., Schlessinger, David, Scott, Robert A., Stöckl, Doris, Visser, Jenny A., Völker, Uwe, Vozzi, Diego, Wilson, James G., Zygmunt, Marek, Boerwinkle, Eric, Buring, Julie E., Crisponi, Laura, Easton, Douglas F., Hayward, Caroline, Hu, Frank B., Liu, Simin, Metspalu, Andres, Pennell, Craig E., Ridker, Paul M., Strauch, Konstantin, Streeten, Elizabeth A., Toniolo, Daniela, Uitterlinden, André G., Ulivi, Sheila, Völzke, Henry, Wareham, Nicholas J., Wellons, Melissa, Franceschini, Nora, Chasman, Daniel I., Thorsteinsdottir, Unnur, Murray, Anna, Stefansson, Kari, Murabito, Joanne M., Ong, Ken K., Perry, John R. B.
Published in Nature communications (04.08.2015)
Published in Nature communications (04.08.2015)
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Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network
Chen, Zhao, Tang, Hua, Qayyum, Rehan, Schick, Ursula M, Nalls, Michael A, Handsaker, Robert, Li, Jin, Lu, Yingchang, Yanek, Lisa R, Keating, Brendan, Meng, Yan, van Rooij, Frank J A, Okada, Yukinori, Kubo, Michiaki, Rasmussen-Torvik, Laura, Keller, Margaux F, Lange, Leslie, Evans, Michele, Bottinger, Erwin P, Linderman, Michael D, Ruderfer, Douglas M, Hakonarson, Hakon, Papanicolaou, George, Zonderman, Alan B, Gottesman, Omri, Thomson, Cynthia, Ziv, Elad, Singleton, Andrew B, Loos, Ruth J F, Sleiman, Patrick M A, Ganesh, Santhi, McCarroll, Steven, Becker, Diane M, Wilson, James G, Lettre, Guillaume, Reiner, Alexander P
Published in Human molecular genetics (15.06.2013)
Published in Human molecular genetics (15.06.2013)
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Journal Article
Generalization and fine mapping of red blood cell trait genetic associations to multi‐ethnic populations: The PAGE study
Hodonsky, Chani J., Schurmann, Claudia, Schick, Ursula M., Kocarnik, Jonathan, Tao, Ran, van Rooij, Frank J. A., Wassel, Christina, Buyske, Steve, Fornage, Myriam, Hindorff, Lucia A., Floyd, James S., Ganesh, Santhi K., Lin, Dan‐Yu, North, Kari E., Reiner, Alex P., Loos, Ruth J. F., Kooperberg, Charles, Avery, Christy L.
Published in American journal of hematology (01.08.2018)
Published in American journal of hematology (01.08.2018)
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Journal Article
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis
Polfus, Linda M., Khajuria, Rajiv K., Schick, Ursula M., Pankratz, Nathan, Pazoki, Raha, Brody, Jennifer A., Chen, Ming-Huei, Auer, Paul L., Floyd, James S., Huang, Jie, Lange, Leslie, van Rooij, Frank J.A., Gibbs, Richard A., Metcalf, Ginger, Muzny, Donna, Veeraraghavan, Narayanan, Walter, Klaudia, Chen, Lu, Yanek, Lisa, Becker, Lewis C., Peloso, Gina M., Wakabayashi, Aoi, Kals, Mart, Metspalu, Andres, Esko, Tõnu, Fox, Keolu, Wallace, Robert, Franceschini, Nora, Matijevic, Nena, Rice, Kenneth M., Bartz, Traci M., Lyytikäinen, Leo-Pekka, Kähönen, Mika, Lehtimäki, Terho, Raitakari, Olli T., Li-Gao, Ruifang, Mook-Kanamori, Dennis O., Lettre, Guillaume, van Duijn, Cornelia M., Franco, Oscar H., Rich, Stephen S., Rivadeneira, Fernando, Hofman, Albert, Uitterlinden, André G., Wilson, James G., Psaty, Bruce M., Soranzo, Nicole, Dehghan, Abbas, Boerwinkle, Eric, Zhang, Xiaoling, Johnson, Andrew D., O’Donnell, Christopher J., Johnsen, Jill M., Reiner, Alexander P., Ganesh, Santhi K., Sankaran, Vijay G.
Published in American journal of human genetics (01.09.2016)
Published in American journal of human genetics (01.09.2016)
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Journal Article
Corrigendum: Rare coding variants and X-linked loci associated with age at menarche
Lunetta, Kathryn L, Day, Felix R, Sulem, Patrick, Ruth, Katherine S, Tung, Joyce Y, Hinds, David A, Esko, Tõnu, Elks, Cathy E, Altmaier, Elisabeth, He, Chunyan, Huffman, Jennifer E, Mihailov, Evelin, Porcu, Eleonora, Robino, Antonietta, Rose, Lynda M, Schick, Ursula M, Stolk, Lisette, Teumer, Alexander, Thompson, Deborah J, Traglia, Michela, Wang, Carol A, Yerges-Armstrong, Laura M, Antoniou, Antonis C, Barbieri, Caterina, Coviello, Andrea D, Cucca, Francesco, Demerath, Ellen W, Dunning, Alison M, Gandin, Ilaria, Grove, Megan L, Gudbjartsson, Daniel F, Hocking, Lynne J, Hofman, Albert, Huang, Jinyan, Jackson, Rebecca D, Karasik, David, Kriebel, Jennifer, Lange, Ethan M, Lange, Leslie A, Langenberg, Claudia, Li, Xin, Luan, Jian'an, Mägi, Reedik, Morrison, Alanna C, Padmanabhan, Sandosh, Pirie, Ailith, Polasek, Ozren, Porteous, David, Reiner, Alex P, Rivadeneira, Fernando, Rudan, Igor, Sala, Cinzia F, Schlessinger, David, Scott, Robert A, Stöckl, Doris, Visser, Jenny A, Völker, Uwe, Vozzi, Diego, Wilson, James G, Zygmunt, Marek, Boerwinkle, Eric, Buring, Julie E, Crisponi, Laura, Easton, Douglas F, Hayward, Caroline, Hu, Frank B, Liu, Simin, Metspalu, Andres, Pennell, Craig E, Ridker, Paul M, Strauch, Konstantin, Streeten, Elizabeth A, Toniolo, Daniela, Uitterlinden, André G, Ulivi, Sheila, Völzke, Henry, Wareham, Nicholas J, Wellons, Melissa, Franceschini, Nora, Chasman, Daniel I, Thorsteinsdottir, Unnur, Murray, Anna, Stefansson, Kari, Murabito, Joanne M, Ong, Ken K, Perry, John R B
Published in Nature communications (17.12.2015)
Published in Nature communications (17.12.2015)
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Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis
van Rooij, Frank J.A., Qayyum, Rehan, Smith, Albert V., Zhou, Yi, Trompet, Stella, Tanaka, Toshiko, Keller, Margaux F., Chang, Li-Ching, Schmidt, Helena, Yang, Min-Lee, Chen, Ming-Huei, Hayes, James, Johnson, Andrew D., Yanek, Lisa R., Mueller, Christian, Lange, Leslie, Floyd, James S., Ghanbari, Mohsen, Zonderman, Alan B., Jukema, J. Wouter, Hofman, Albert, van Duijn, Cornelia M., Desch, Karl C., Saba, Yasaman, Ozel, Ayse B., Snively, Beverly M., Wu, Jer-Yuarn, Schmidt, Reinhold, Fornage, Myriam, Klein, Robert J., Fox, Caroline S., Matsuda, Koichi, Kamatani, Naoyuki, Wild, Philipp S., Stott, David J., Ford, Ian, Slagboom, P. Eline, Yang, Jaden, Chu, Audrey Y., Lambert, Amy J., Uitterlinden, André G., Franco, Oscar H., Hofer, Edith, Ginsburg, David, Hu, Bella, Keating, Brendan, Schick, Ursula M., Brody, Jennifer A., Li, Jun Z., Chen, Zhao, Zeller, Tanja, Guralnik, Jack M., Chasman, Daniel I., Peters, Luanne L., Kubo, Michiaki, Becker, Diane M., Li, Jin, Eiriksdottir, Gudny, Rotter, Jerome I., Levy, Daniel, Grossmann, Vera, Patel, Kushang V., Chen, Chien-Hsiun, Ridker, Paul M., Tang, Hua, Launer, Lenore J., Rice, Kenneth M., Li-Gao, Ruifang, Ferrucci, Luigi, Evans, Michelle K., Choudhuri, Avik, Trompouki, Eirini, Abraham, Brian J., Yang, Song, Takahashi, Atsushi, Kamatani, Yoichiro, Kooperberg, Charles, Harris, Tamara B., Jee, Sun Ha, Coresh, Josef, Tsai, Fuu-Jen, Longo, Dan L., Chen, Yuan-Tsong, Felix, Janine F., Yang, Qiong, Psaty, Bruce M., Boerwinkle, Eric, Becker, Lewis C., Mook-Kanamori, Dennis O., Wilson, James G., Gudnason, Vilmundur, O'Donnell, Christopher J., Dehghan, Abbas, Cupples, L. Adrienne, Nalls, Michael A., Morris, Andrew P., Okada, Yukinori, Reiner, Alexander P., Zon, Leonard I., Ganesh, Santhi K.
Published in American journal of human genetics (05.01.2017)
Published in American journal of human genetics (05.01.2017)
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Correction: Risk Factors Associated With Epidural Use
Lancaster, Samuel M, Schick, Ursula M, Osman, Morwan M, Enquobahrie, Daniel A
Published in Journal of clinical medicine research (01.08.2016)
Published in Journal of clinical medicine research (01.08.2016)
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Risk factors associated with epidural use
Lancaster, Samuel M, Schick, Ursula M, Osman, Morwan M, Enquobahrie, Daniel A
Published in Journal of clinical medicine research (01.04.2012)
Published in Journal of clinical medicine research (01.04.2012)
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Interleukin-6 Signaling Effects on Ischemic Stroke and Other Cardiovascular Outcomes: A Mendelian Randomization Study
Georgakis, Marios K, Malik, Rainer, Gill, Dipender, Franceschini, Nora, Sudlow, Cathie L M, Dichgans, Martin
Published in Circulation. Genomic and precision medicine (01.06.2020)
Published in Circulation. Genomic and precision medicine (01.06.2020)
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SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function
Li, Man, Li, Yong, Weeks, Olivia, Mijatovic, Vladan, Teumer, Alexander, Huffman, Jennifer E, Tromp, Gerard, Fuchsberger, Christian, Gorski, Mathias, Lyytikäinen, Leo-Pekka, Nutile, Teresa, Sedaghat, Sanaz, Sorice, Rossella, Tin, Adrienne, Yang, Qiong, Ahluwalia, Tarunveer S, Arking, Dan E, Bihlmeyer, Nathan A, Böger, Carsten A, Carroll, Robert J, Chasman, Daniel I, Cornelis, Marilyn C, Dehghan, Abbas, Faul, Jessica D, Feitosa, Mary F, Gambaro, Giovanni, Gasparini, Paolo, Giulianini, Franco, Heid, Iris, Huang, Jinyan, Imboden, Medea, Jackson, Anne U, Jeff, Janina, Jhun, Min A, Katz, Ronit, Kifley, Annette, Kilpeläinen, Tuomas O, Kumar, Ashish, Laakso, Markku, Li-Gao, Ruifang, Lohman, Kurt, Lu, Yingchang, Mägi, Reedik, Malerba, Giovanni, Mihailov, Evelin, Mohlke, Karen L, Mook-Kanamori, Dennis O, Robino, Antonietta, Ruderfer, Douglas, Salvi, Erika, Schick, Ursula M, Schulz, Christina-Alexandra, Smith, Albert V, Smith, Jennifer A, Traglia, Michela, Yerges-Armstrong, Laura M, Zhao, Wei, Goodarzi, Mark O, Kraja, Aldi T, Liu, Chunyu, Wessel, Jennifer, Boerwinkle, Eric, Borecki, Ingrid B, Bork-Jensen, Jette, Bottinger, Erwin P, Braga, Daniele, Brandslund, Ivan, Brody, Jennifer A, Campbell, Archie, Carey, David J, Christensen, Cramer, Coresh, Josef, Crook, Errol, Curhan, Gary C, Cusi, Daniele, de Boer, Ian H, de Vries, Aiko P J, Denny, Joshua C, Devuyst, Olivier, Dreisbach, Albert W, Endlich, Karlhans, Esko, Tõnu, Franco, Oscar H, Fulop, Tibor, Gerhard, Glenn S, Glümer, Charlotte, Gottesman, Omri, Grarup, Niels, Gudnason, Vilmundur, Hansen, Torben, Harris, Tamara B, Hayward, Caroline, Hocking, Lynne, Hofman, Albert, Hu, Frank B, Husemoen, Lise Lotte N, Jackson, Rebecca D, Jørgensen, Torben, Jørgensen, Marit E, Kähönen, Mika
Published in Journal of the American Society of Nephrology (01.03.2017)
Published in Journal of the American Society of Nephrology (01.03.2017)
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Rare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African Americans
Olfson, E, Saccone, N L, Johnson, E O, Chen, L-S, Culverhouse, R, Doheny, K, Foltz, S M, Fox, L, Gogarten, S M, Hartz, S, Hetrick, K, Laurie, C C, Marosy, B, Amin, N, Arnett, D, Barr, R G, Bartz, T M, Bertelsen, S, Borecki, I B, Brown, M R, Chasman, D I, van Duijn, C M, Feitosa, M F, Fox, E R, Franceschini, N, Franco, O H, Grove, M L, Guo, X, Hofman, A, Kardia, S L R, Morrison, A C, Musani, S K, Psaty, B M, Rao, D C, Reiner, A P, Rice, K, Ridker, P M, Rose, L M, Schick, U M, Schwander, K, Uitterlinden, A G, Vojinovic, D, Wang, J-C, Ware, E B, Wilson, G, Yao, J, Zhao, W, Breslau, N, Hatsukami, D, Stitzel, J A, Rice, J, Goate, A, Bierut, L J
Published in Molecular psychiatry (01.05.2016)
Published in Molecular psychiatry (01.05.2016)
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